Methantheline
This anticholinergic drug blocks muscarinic receptors in the gut and bladder, reducing smooth muscle spasms and secretions, making it useful for treating peptic ulcers, irritable bowel syndrome, and excessive sweating. It has been largely replaced by more selective and better-tolerated medications.
分子量
340.4000 g/mol
LogP
3.30
TPSA
35.50 Ų
リピンスキーの五則
適合
作用機序
Increases water content in the intestinal lumen through osmotic or stimulant mechanisms, promoting bowel motility and facilitating defecation.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Increases water content in the intestinal lumen through osmotic or stimulant mechanisms, promoting bowel motility and facilitating defecation.
2D構造
Cite this structure
Embed this structure
SMILES
CC[N+](C)(CC)CCOC(=O)C1c2ccccc2Oc2ccccc21
InChI
InChI=1S/C21H26NO3/c1-4-22(3,5-2)14-15-24-21(23)20-16-10-6-8-12-18(16)25-19-13-9-7-11-17(19)20/h6-13,20H,4-5,14-15H2,1-3H3/q+1
Molecular Formula
C21H26NO3+
HBD / HBA
- / 3
回転可能結合数
7
重原子数
25
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
よくある質問
This anticholinergic drug blocks muscarinic receptors in the gut and bladder, reducing smooth muscle spasms and secretions, making it useful for treating peptic ulcers, irritable bowel syndrome, and excessive sweating. It has been largely replaced by more selective and better-tolerated medications.
Increases water content in the intestinal lumen through osmotic or stimulant mechanisms, promoting bowel motility and facilitating defecation.
Yes, Methantheline is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1201264. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 4097. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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